Evidence map›Paper›PMID 29972436›Full record

ArticleClinics (Sao Paulo, Brazil)2018

Prophylactic application of laser light restores L-FABP expression in the livers of rats submitted to partial ischemia.

Kelvin Henrique Vilalva, Rebeca Lopes Figueira, Marina Silveira, Catarina Graf, Frances Lanhellas Gonçalves, Lourenço Sbragia, Maria Cecília Gomes, Fabrícia Mumic, José Dirceu Vollet-Filho, Vanderlei Salvador Bagnato and 2 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in Clinics (Sao Paulo, Brazil), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Kelvin Henrique VilalvaDivisao de Transplante de Figado, Departamento de Cirurgia e Anatomia, Faculdade de Medicina de Ribeirao Preto, Universidade de Sao Paulo, Ribeirao Preto, SP, BR.
Rebeca Lopes FigueiraLaboratorio de Cirurgia Fetal Experimental, Divisao de Cirurgia Pediatrica, Departamento de Cirurgia e Anatomia, Faculdade de Medicina de Ribeirao Preto, Universidade de Sao Paulo, Ribeirao Preto, SP, BR.
Marina SilveiraDivisao de Transplante de Figado, Departamento de Cirurgia e Anatomia, Faculdade de Medicina de Ribeirao Preto, Universidade de Sao Paulo, Ribeirao Preto, SP, BR.
Catarina GrafDivisao de Transplante de Figado, Departamento de Cirurgia e Anatomia, Faculdade de Medicina de Ribeirao Preto, Universidade de Sao Paulo, Ribeirao Preto, SP, BR.
Frances Lanhellas GonçalvesLaboratorio de Cirurgia Fetal Experimental, Divisao de Cirurgia Pediatrica, Departamento de Cirurgia e Anatomia, Faculdade de Medicina de Ribeirao Preto, Universidade de Sao Paulo, Ribeirao Preto, SP, BR.
Lourenço SbragiaLaboratorio de Cirurgia Fetal Experimental, Divisao de Cirurgia Pediatrica, Departamento de Cirurgia e Anatomia, Faculdade de Medicina de Ribeirao Preto, Universidade de Sao Paulo, Ribeirao Preto, SP, BR.
Maria Cecília GomesDivisao de Transplante de Figado, Departamento de Cirurgia e Anatomia, Faculdade de Medicina de Ribeirao Preto, Universidade de Sao Paulo, Ribeirao Preto, SP, BR.
Fabrícia MumicDivisao de Transplante de Figado, Departamento de Cirurgia e Anatomia, Faculdade de Medicina de Ribeirao Preto, Universidade de Sao Paulo, Ribeirao Preto, SP, BR.
José Dirceu Vollet-FilhoDepartamento de Fisica e Ciencia dos Materiais, Instituto de Fisica de Sao Carlos, Universidade de Sao Paulo, Sao Carlos, SP, BR.
Vanderlei Salvador BagnatoDepartamento de Fisica e Ciencia dos Materiais, Instituto de Fisica de Sao Carlos, Universidade de Sao Paulo, Sao Carlos, SP, BR.
Luiz Augusto Carneiro D'AlbuquerqueDepartamento de Gastroenterologia, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, SP, BR.
Orlando Castro-E-SilvaDivisao de Transplante de Figado, Departamento de Cirurgia e Anatomia, Faculdade de Medicina de Ribeirao Preto, Universidade de Sao Paulo, Ribeirao Preto, SP, BR.
Universidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe objective of the present study was to evaluate the protective effect of pre-conditioning treatment with laser light on hepatic injury in rats submitted to partial ischemia using mitochondrial function and liver fatty acid binding protein as markers.

methodsRats were divided into four groups (n=5): 1) Control, 2) Control + Laser, 3) Partial Ischemia and 4) Partial Ischemia + Laser. Ischemia was induced by clamping the hepatic pedicle of the left and middle lobes of the liver for 60 minutes. Laser light at 660 nm was applied to the liver immediately prior to the induction of ischemia at 22.5 J/cm2, with 30 seconds of illumination at five individual points. The animals were sacrificed after 30 minutes of reperfusion. Blood and liver tissues were collected for analysis of mitochondrial function, determination of malondialdehyde and analysis of fatty acid binding protein expression by Western blot.

resultsMitochondrial function decreased in the Partial Ischemia group, especially during adenosine diphosphate-activated respiration (state 3), and the expression of fatty acid binding protein was also reduced. The application of laser light prevented bioenergetic changes and restored the expression of fatty acid binding protein.

conclusionProphylactic application of laser light to the livers of rats submitted to partial ischemia was found to have a protective effect in the liver, with normalization of both mitochondrial function and fatty acid binding protein tissue expression.

Indexed as

Alanine TransaminaseAnimalsAspartate AminotransferasesBlotting, WesternFatty Acid-Binding ProteinsIschemic PreconditioningLiverLow-Level Light TherapyMalondialdehydeMitochondrial MembranesMitochondrial SwellingRats, WistarReperfusion InjuryReproducibility of ResultsAlanine TransaminaseAspartate AminotransferasesFabp1 protein, mouseFatty Acid-Binding ProteinsMalondialdehyde

Identifiers

PMID29972436
PMCPMC6005990
OpenAlexW2883376683

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.